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Classification, diagnosis and potential mechanisms in Pontocerebellar Hypoplasia

Pontocerebellar Hypoplasia (PCH) is group of very rare, inherited progressive neurodegenerative disorders with prenatal onset. Up to now seven different subtypes have been reported (PCH1-7). The incidence of each subtype is unknown. All subtypes share common characteristics, including hypoplasia/atr...

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書目詳細資料
Main Authors: Namavar, Yasmin, Barth, Peter G, Poll-The, Bwee Tien, Baas, Frank
格式: Artigo
語言:Inglês
出版: BioMed Central 2011
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3159098/
https://ncbi.nlm.nih.gov/pubmed/21749694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-50
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